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Published on: July 7, 2014
Resveratrol affects CYP1A expression in rainbow trout hepatocytes
Neelakanteswar Aluru1, Mathilakath M Vijayan
1Department of Biology, University of Waterloo, Waterloo, Ont., Canada, N2L 3G1.
Aquatic Toxicology (Amsterdam, Netherlands)
|February 10, 2006
Summary
Resveratrol (RVT) acts as an aryl hydrocarbon receptor (AhR) antagonist in rainbow trout, but unexpectedly induces CYP1A expression at lower doses. This study evaluates RVT
Area of Science:
- Environmental Toxicology
- Biochemistry
- Aquatic Toxicology
Background:
- Resveratrol (RVT) is a known aryl hydrocarbon receptor (AhR) antagonist in mammals.
- A reliable AhR antagonist is needed for research in rainbow trout (Oncorhynchus mykiss).
Purpose of the Study:
- To evaluate Resveratrol (RVT) as an AhR antagonist in rainbow trout hepatocytes.
- To investigate the dose-dependent effects of RVT on AhR signaling and CYP1A expression.
Main Methods:
- Primary trout hepatocytes were cultured and exposed to varying doses of RVT and beta-naphthoflavone (BNF).
- CYP1A and AhR protein expression were measured.
- Transcriptional and translational inhibitors (actinomycin D, cycloheximide) were used to elucidate mechanisms.
- CYP1A1 mRNA levels were quantified.
Main Results:
- BNF increased CYP1A and AhR protein, an effect inhibited by high doses of RVT (10(-5)-10(-7) M).
- Low doses of RVT (10(-8)-10(-10) M) alone significantly increased CYP1A protein expression.
- RVT's induction of CYP1A was regulated transcriptionally and translationally.
- Low-dose RVT (10(-9) M) increased CYP1A1 mRNA in BNF-primed hepatocytes.
Conclusions:
- Resveratrol functions as an AhR antagonist in trout hepatocytes.
- RVT exhibits a dual role, antagonizing AhR at high concentrations and inducing CYP1A expression at lower concentrations (<10(-8) M).
- These findings highlight the complex effects of RVT in piscine systems and its potential as a research tool.

